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Human Reproduction Update|August 28, 1999
Glycosylation of G-protein-coupled receptors for hormones central to normal reproductive functioning: its occurrence and roleM Wheatley, S R HawtinThe Biochemical Journal|February 15, 2001
Identification of an extracellular segment of the oxytocin receptor providing agonist-specific binding epitopesS R Hawtin, H C Howard, M WheatleyJournal of Neurochemistry|July 1, 1995
The intracellular component of cellular 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) reduction is specifically inhibited by beta-amyloid peptidesM S Shearman, S R Hawtin, V J TailorThe Biochemical Journal|June 21, 2001
Identification of the glycosylation sites utilized on the V1a vasopressin receptor and assessment of their role in receptor signalling and expressionS R Hawtin, A R Davies, G Matthews, et al.The Journal of Biological Chemistry|July 24, 2001
Palmitoylation of the vasopressin V1a receptor reveals different conformational requirements for signaling, agonist-induced receptor phosphorylation, and sequestrationS R Hawtin, A B Tobin, S Patel, et al.Biochemistry|November 7, 2000
Critical role of a subdomain of the N-terminus of the V1a vasopressin receptor for binding agonists but not antagonists; functional rescue by the oxytocin receptor N-terminusS R Hawtin, V J Wesley, R A Parslow, et al.Neuroscience Letters|January 23, 1995
Sulfated glycosaminoglycans and dyes attenuate the neurotoxic effects of beta-amyloid in rat PC12 cellsS J Pollack, I I Sadler, S R Hawtin, et al.Neuroscience Letters|September 15, 1995
Sulfonated dyes attenuate the toxic effects of beta-amyloid in a structure-specific fashionS J Pollack, I I Sadler, S R Hawtin, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 1, 1997
Chimeric strategies for the rational design of bioactive analogs of small peptide hormonesJ Howl, U Langel, S R Hawtin, et al.Cell Calcium|May 7, 2002
Curcumin: a new cell-permeant inhibitor of the inositol 1,4,5-trisphosphate receptorJ L Dyer, S Zafar Khan, J G Bilmen, et al.Pageof 2